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Mapping the impact of patient and public involvement on health and social care research: a systematic review

Health expectations : an international journal of public participation in health care and health policy, 2014-10, Vol.17 (5), p.637-650

2014

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The GRIPP checklist: Strengthening the quality of patient and public involvement reporting in research

International journal of technology assessment in health care, 2011-10, Vol.27 (4), p.391-399

2011

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A systematic mapping review of effective interventions for communicating with, supporting and providing information to parents of preterm infants

BMJ open, 2011-01, Vol.1 (1), p.e000023-e000023

2011

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Impact of patient and public (PPI) involvement in the Life After Prostate Cancer Diagnosis (LAPCD) study: a mixed-methods study

BMJ open, 2022-11, Vol.12 (11), p.e060861-e060861

2022

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Examining the levels of psychological support available to patients with haematological cancer in England: a mixed methods study

BMJ open, 2023-02, Vol.13 (2), p.e060106-e060106

2023

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Electronic cigarettes as a smoking cessation aid for patients with cancer: beliefs and behaviours of clinicians in the UK

BMJ open, 2020-11, Vol.10 (11), p.e037637-e037637

2020

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The impact of the COVID-19 pandemic on nursing students’ navigation of their nursing programmes and experiences of resilience. A qualitative study

International journal of nursing studies advances, 2023-12, Vol.5, p.100146-100146, Article 100146

2023

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The psychosocial experiences of head and neck cancer caregivers following (chemo)radiotherapy: A systematic qualitative review and narrative synthesis

Psycho-oncology (Chichester, England), 2023-10, Vol.32 (10), p.1469-1480

2023

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Psychometric properties of the Beliefs about Medicine Questionnaire–adjuvant endocrine therapy (BMQ-AET) for women taking AETs following early-stage breast cancer

Health psychology open, 2017-07, Vol.4 (2), p.2055102917740469-2055102917740469

2017

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A Systematic Review of the Impact of Patient and Public Involvement on Service Users, Researchers and Communities

The patient : patient-centered outcomes research, 2014-12, Vol.7 (4), p.387-395

2014

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The psychosocial experiences of human papillomavirus (HPV) positive oropharyngeal cancer patients following (chemo)radiotherapy: A systematic review and meta‐ethnography

Psycho-oncology (Chichester, England), 2022-12, Vol.31 (12), p.2009-2019

2022

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If They'd Said You Should Only Drink Five Units I'd Have Listened: A Mixed Methods Study of Alcohol Consumption Following a Diagnosis of Breast Cancer

Psycho-oncology (Chichester, England), 2024-08, Vol.33 (8), p.e9305-n/a

2024

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Shouldn't We Know This Already? UK Women's Views About Communicating the Link Between Alcohol Consumption and Risk of Breast Cancer

Health communication, 2024-08, Vol.39 (9), p.1866-1876

2024

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SUPPORTING WOMEN WITH ADHERENCE TO ADJUVANT ENDOCRINE THERAPY – RESULTS FROM THE SWEET FEASIBILITY STUDY

European journal of surgical oncology, 2024-05, Vol.50, p.108079, Article 108079

2024

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A systematic review to explore the effectiveness of physical health and psychosocial interventions on anxiety, depression and quality of life in people living with blood cancer

Journal of psychosocial oncology, 2024, Vol.42 (1), p.113-147

2024

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What if something goes wrong? A grounded theory study of parents’ decision-making processes around mode of breech birth at term gestation

Midwifery, 2019-11, Vol.78, p.114-122

2019

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Patient and public engagement in health-related quality of life and patient-reported outcomes research: what is important and why should we care? Findings from the first ISOQOL patient engagement symposium

Quality of life research, 2015-05, Vol.24 (5), p.1069-1076

2015

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Optimising patient-initiated follow-up care – A qualitative analysis of women with breast cancer in the UK

European journal of oncology nursing : the official journal of European Oncology Nursing Society, 2022-10, Vol.60, p.102183-102183, Article 102183

2022

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Exploring lessons from Covid‐19 for the role of the voluntary sector in integrated care systems

Health & social care in the community, 2022-11, Vol.30 (6), p.e6689-e6698

2022

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Strategies for living well with hormone-responsive advanced prostate cancer—a qualitative exploration

Supportive care in cancer, 2021-03, Vol.29 (3), p.1317-1325

2021

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A Qualitative Exploration of Prostate Cancer Survivors Experiencing Psychological Distress: Loss of Self, Function, Connection, and Control

Oncology nursing forum, 2020-05, Vol.47 (3), p.318-330

2020

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Development of the ‘ACT now & check-it-out’ intervention to support patient-initiated follow up for Head and Neck cancer patients

Patient education and counseling, 2024-02, Vol.119, p.108033-108033, Article 108033

2024

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Patient and Public Involvement in Patient-Reported Outcome Measures: Evolution Not Revolution

The patient : patient-centered outcomes research, 2012, Vol.5 (2), p.79-87

2012

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Experiences of Support for Sexual Dysfunction in Men With Prostate Cancer: Findings From a U.K.-Wide Mixed Methods Study

Journal of sexual medicine, 2021-03, Vol.18 (3), p.515-525

2021

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‘Very difficult for an ordinary guy’: Factors influencing the quality of treatment decision-making amongst men diagnosed with localised and locally advanced prostate cancer: Findings from a UK-wide mixed methods study

Patient education and counseling, 2019-04, Vol.102 (4), p.797-803

2019

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Mapping the impact of patient and public involvement on health and social care research: a systematic review

The GRIPP checklist: Strengthening the quality of patient and public involvement reporting in research

A systematic mapping review of effective interventions for communicating with, supporting and providing information to parents of preterm infants

Impact of patient and public (PPI) involvement in the Life After Prostate Cancer Diagnosis (LAPCD) study: a mixed-methods study

Examining the levels of psychological support available to patients with haematological cancer in England: a mixed methods study

Electronic cigarettes as a smoking cessation aid for patients with cancer: beliefs and behaviours of clinicians in the UK

The impact of the COVID-19 pandemic on nursing students’ navigation of their nursing programmes and experiences of resilience. A qualitative study

The psychosocial experiences of head and neck cancer caregivers following (chemo)radiotherapy: A systematic qualitative review and narrative synthesis

Psychometric properties of the Beliefs about Medicine Questionnaire–adjuvant endocrine therapy (BMQ-AET) for women taking AETs following early-stage breast cancer

A Systematic Review of the Impact of Patient and Public Involvement on Service Users, Researchers and Communities

The psychosocial experiences of human papillomavirus (HPV) positive oropharyngeal cancer patients following (chemo)radiotherapy: A systematic review and meta‐ethnography

If They'd Said You Should Only Drink Five Units I'd Have Listened: A Mixed Methods Study of Alcohol Consumption Following a Diagnosis of Breast Cancer

Shouldn't We Know This Already? UK Women's Views About Communicating the Link Between Alcohol Consumption and Risk of Breast Cancer

SUPPORTING WOMEN WITH ADHERENCE TO ADJUVANT ENDOCRINE THERAPY – RESULTS FROM THE SWEET FEASIBILITY STUDY

A systematic review to explore the effectiveness of physical health and psychosocial interventions on anxiety, depression and quality of life in people living with blood cancer

What if something goes wrong? A grounded theory study of parents’ decision-making processes around mode of breech birth at term gestation

Patient and public engagement in health-related quality of life and patient-reported outcomes research: what is important and why should we care? Findings from the first ISOQOL patient engagement symposium

Optimising patient-initiated follow-up care – A qualitative analysis of women with breast cancer in the UK

Exploring lessons from Covid‐19 for the role of the voluntary sector in integrated care systems

Strategies for living well with hormone-responsive advanced prostate cancer—a qualitative exploration

A Qualitative Exploration of Prostate Cancer Survivors Experiencing Psychological Distress: Loss of Self, Function, Connection, and Control

Development of the ‘ACT now & check-it-out’ intervention to support patient-initiated follow up for Head and Neck cancer patients

Patient and Public Involvement in Patient-Reported Outcome Measures: Evolution Not Revolution

Experiences of Support for Sexual Dysfunction in Men With Prostate Cancer: Findings From a U.K.-Wide Mixed Methods Study

‘Very difficult for an ordinary guy’: Factors influencing the quality of treatment decision-making amongst men diagnosed with localised and locally advanced prostate cancer: Findings from a UK-wide mixed methods study

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